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Updated: Mar 31, 2026

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq
Published on: March 12, 2021
SC-MO-GRN-DB: A comprehensive repository for single-cell multiomic gene regulatory networks
Hannah Valensi1, Karamveer Karamveer1, Eric Moeller1
1Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA, USA.
We created SC-MO-GRN-DB, a database of gene regulatory networks (GRNs) and single-cell multiomic data. This resource aids in developing and validating GRN inference methods using epigenetic and transcriptomic information.
Area of Science:
- Genomics
- Systems Biology
- Bioinformatics
Background:
- Gene regulatory networks (GRNs) are crucial for understanding cellular processes.
- Current GRN resources often lack epigenetic data, hindering method development.
- There is a need for comprehensive datasets integrating multiple molecular layers.
Purpose of the Study:
- To develop SC-MO-GRN-DB, a database linking experimentally validated GRNs with single-cell multiomic data.
- To provide a platform for benchmarking and validating GRN inference algorithms.
- To facilitate the study of gene regulation across diverse human and mouse tissues.
Main Methods:
- Curated high-confidence experimental datasets to build ground-truth GRNs.
- Integrated single-cell data from six modalities: scRNA-seq, scATAC-seq, scChIP-seq, scDNA-Met, scHi-C, and scCRISPR-seq.
- Compiled over 22 million regulatory edges and processed more than two million single cells.
Main Results:
- Established SC-MO-GRN-DB, a comprehensive repository of GRNs and multiomic single-cell data.
- Included over 22 million experimentally validated regulatory edges.
- Integrated multiomic data from over two million cells across six molecular modalities.
Conclusions:
- SC-MO-GRN-DB offers a unique resource for advancing GRN research.
- The database enables robust development and validation of GRN inference methods.
- Facilitates deeper understanding of gene regulation by integrating multiomic and epigenetic data.
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